JPH041734B2 - - Google Patents
Info
- Publication number
- JPH041734B2 JPH041734B2 JP30378386A JP30378386A JPH041734B2 JP H041734 B2 JPH041734 B2 JP H041734B2 JP 30378386 A JP30378386 A JP 30378386A JP 30378386 A JP30378386 A JP 30378386A JP H041734 B2 JPH041734 B2 JP H041734B2
- Authority
- JP
- Japan
- Prior art keywords
- acetic acid
- methyl acetate
- column
- liquid
- solvent
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
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- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 126
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims description 38
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 claims description 38
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 28
- 239000002904 solvent Substances 0.000 claims description 23
- 238000006243 chemical reaction Methods 0.000 claims description 21
- 238000004821 distillation Methods 0.000 claims description 21
- 238000000605 extraction Methods 0.000 claims description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 19
- 238000007254 oxidation reaction Methods 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 16
- 239000012452 mother liquor Substances 0.000 claims description 14
- 239000007788 liquid Substances 0.000 claims description 13
- URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 claims description 12
- 230000018044 dehydration Effects 0.000 claims description 12
- 238000006297 dehydration reaction Methods 0.000 claims description 12
- 239000007789 gas Substances 0.000 claims description 11
- 239000007791 liquid phase Substances 0.000 claims description 10
- 239000003054 catalyst Substances 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 9
- 239000006227 byproduct Substances 0.000 claims description 7
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 6
- 229910001882 dioxygen Inorganic materials 0.000 claims description 5
- 239000007795 chemical reaction product Substances 0.000 claims description 4
- 230000003647 oxidation Effects 0.000 claims description 4
- 239000012071 phase Substances 0.000 description 6
- 229910001385 heavy metal Inorganic materials 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 238000011437 continuous method Methods 0.000 description 3
- 239000012153 distilled water Substances 0.000 description 3
- 238000000622 liquid--liquid extraction Methods 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 238000000638 solvent extraction Methods 0.000 description 3
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- MTJGVAJYTOXFJH-UHFFFAOYSA-N 3-aminonaphthalene-1,5-disulfonic acid Chemical compound C1=CC=C(S(O)(=O)=O)C2=CC(N)=CC(S(O)(=O)=O)=C21 MTJGVAJYTOXFJH-UHFFFAOYSA-N 0.000 description 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
- ICWYLDBGAYSGDZ-UHFFFAOYSA-N acetic acid methyl acetate Chemical compound CC(O)=O.CC(O)=O.COC(C)=O ICWYLDBGAYSGDZ-UHFFFAOYSA-N 0.000 description 1
- IBGCCZDQQQOZLD-UHFFFAOYSA-N acetic acid methyl acetate hydrate Chemical compound O.CC(O)=O.COC(C)=O IBGCCZDQQQOZLD-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- -1 bromine compound Chemical class 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 150000001845 chromium compounds Chemical class 0.000 description 1
- 229940011182 cobalt acetate Drugs 0.000 description 1
- 150000001869 cobalt compounds Chemical class 0.000 description 1
- QAHREYKOYSIQPH-UHFFFAOYSA-L cobalt(II) acetate Chemical compound [Co+2].CC([O-])=O.CC([O-])=O QAHREYKOYSIQPH-UHFFFAOYSA-L 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 150000002506 iron compounds Chemical class 0.000 description 1
- 150000002697 manganese compounds Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 239000011268 mixed slurry Substances 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 150000002816 nickel compounds Chemical class 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 150000003682 vanadium compounds Chemical class 0.000 description 1
- 239000002918 waste heat Substances 0.000 description 1
Landscapes
- Heat Treatment Of Water, Waste Water Or Sewage (AREA)
- Extraction Or Liquid Replacement (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
【発明の詳細な説明】
＜産業上の利用分野＞
本発明はテレフタル酸製造過程において溶媒と
して用いる酢酸の回収方法に関し、特に水中に含
まれ損失する酢酸を回収する方法に関するもので
ある。DETAILED DESCRIPTION OF THE INVENTION <Industrial Application Field> The present invention relates to a method for recovering acetic acid used as a solvent in the process of producing terephthalic acid, and particularly to a method for recovering acetic acid contained in water and lost.
＜従来の技術＞
パラキシレンを触媒の存在下、酢酸溶媒中で分
子状酸素含有ガスにより液相酸化してテレフタル
酸を製造する方法によつて得られるスラリー状の
酸化反応生成物からテレフタル酸を分離した反応
母液から酢酸を回収するに当たり、例えば、該反
応母液を蒸留して、溶媒−水混合液を得、続いて
該混合液を溶媒脱水蒸留塔に導入して溶媒を回収
することは公知である（特開昭51−63369号公
報）。<Prior art> Terephthalic acid is produced from a slurry-like oxidation reaction product obtained by a method of producing terephthalic acid by liquid-phase oxidation of paraxylene with a molecular oxygen-containing gas in an acetic acid solvent in the presence of a catalyst. It is known that in recovering acetic acid from the separated reaction mother liquor, for example, the reaction mother liquor is distilled to obtain a solvent-water mixture, and then the mixture is introduced into a solvent dehydration distillation column to recover the solvent. (Japanese Unexamined Patent Publication No. 1983-63369).
＜発明が解決しようとする問題点＞
しかしながら、この方法は溶媒である酢酸が、
その中に含まれる水分を蒸留除去する工程で損失
するという問題があり、その為溶媒の原単位が高
くなるという欠点がある。<Problems to be solved by the invention> However, in this method, the solvent acetic acid is
There is a problem in that the water contained therein is lost in the process of distilling and removing it, resulting in a disadvantage that the unit consumption of the solvent becomes high.
＜問題点を解決するための手段および作用＞
そこで、本発明者らは上記実情に鑑がみ、酢酸
から水分を除去する脱水蒸留塔の留出水に微量含
まれる酢酸を回収する方法について鋭意研究した
結果、パラキシレンの酸化反応の際、溶媒である
酢酸から副生する酢酸メチルを用いて液−液抽出
することにより有効に回収できることを見出し、
本発明を完成させた。<Means and effects for solving the problems> Therefore, in view of the above-mentioned circumstances, the present inventors have made efforts to recover a trace amount of acetic acid contained in distilled water from a dehydration distillation column that removes water from acetic acid. As a result of research, we discovered that para-xylene can be effectively recovered by liquid-liquid extraction using methyl acetate, which is a by-product, from the solvent acetic acid during the oxidation reaction.
The present invention has been completed.
すなわち、本発明はパラキシレンを酢酸溶媒
中、触媒の存在下分子状酸素含有ガスで液相酸化
してテレフタル酸を製造する方法によつて得られ
るスラリー状の酸化反応生成物からテレフタル酸
を分離した反応母液から酢酸を回収するに当た
り、該反応母液を脱水蒸留塔に導入して、塔下部
から酢酸を回収し、塔上部から水を主体とし、酢
酸−酢酸メチルを含む混合液を留出せしめた後、
該混合液中に微量含まれる酢酸を、液相酸化反応
で酢酸から副生した回収酢酸メチルを主体とする
抽出溶媒を用いて液−液抽出することにより回収
することを特徴とする酢酸の回収方法である。 That is, the present invention separates terephthalic acid from a slurry-like oxidation reaction product obtained by a method of producing terephthalic acid by liquid-phase oxidation of para-xylene with a molecular oxygen-containing gas in the presence of a catalyst in an acetic acid solvent. To recover acetic acid from the reaction mother liquor, the reaction mother liquor is introduced into a dehydration distillation column, acetic acid is recovered from the lower part of the column, and a mixed liquid mainly composed of water and containing acetic acid and methyl acetate is distilled from the upper part of the column. After
Recovery of acetic acid, characterized in that a trace amount of acetic acid contained in the mixed liquid is recovered by liquid-liquid extraction using an extraction solvent mainly composed of recovered methyl acetate produced as a by-product from acetic acid in a liquid phase oxidation reaction. It's a method.
以下、本発明を詳細に説明する。 The present invention will be explained in detail below.
本発明で用いられるテレフタル酸の製造方法と
しては、パラキシレンを酢酸溶媒中、触媒の存在
下、分子状酸素含有ガスで、液相酸化してテレフ
タル酸を製造する方法であればどの様な方法でも
よい。 As a method for producing terephthalic acid used in the present invention, any method can be used as long as paraxylene is oxidized in an acetic acid solvent in the presence of a catalyst in a liquid phase with a gas containing molecular oxygen to produce terephthalic acid. But that's fine.
触媒としては、重金属化合物単独系が通常用い
られる。反応促進剤は使用しても、しなくてもよ
く使用する場合は公知のアセトアルデヒド、メチ
ルエチルケトン、パラアルデヒド、または臭素化
合物などが選ばれる。重金属触媒としては、通
常、コバルト化合物、さらに必要に応じて、バナ
ジウム化合物、クロム化合物、マンガン化合物、
鉄化合物、ニツケル化合物が用いられる。触媒の
使用量は重金属触媒が、通常、酢酸に対して0.01
〜1.0重量％であり、反応促進剤を使用する場合
には反応促進剤の使用量は重金属に対して１〜10
重量倍である。反応温度は、通常、120〜275℃で
ある。分子状酸素含有ガスとしては、純酸素や工
業排ガスも使用可能であるが、工業的には通常の
空気が用いられる。反応系中の酸素分圧、全反応
圧力が１〜50気圧の範囲で、排ガス中の酸素濃度
が１〜８％の範囲になるように操作するのが好ま
しい。反応方式としては回分式、半連続式、連続
式のいずれも採用できるが、連続式が好ましく用
いられる。 As the catalyst, a heavy metal compound alone is usually used. A reaction accelerator may or may not be used. When used, a known acetaldehyde, methyl ethyl ketone, paraaldehyde, or a bromine compound is selected. The heavy metal catalyst is usually a cobalt compound, and if necessary, a vanadium compound, a chromium compound, a manganese compound,
Iron compounds and nickel compounds are used. The amount of catalyst used is usually 0.01 of heavy metal catalyst per acetic acid.
~1.0% by weight, and if a reaction accelerator is used, the amount of reaction accelerator used is 1 to 10% by weight relative to the heavy metal.
It is twice the weight. The reaction temperature is usually 120-275°C. Although pure oxygen or industrial exhaust gas can be used as the molecular oxygen-containing gas, ordinary air is used industrially. It is preferable to operate so that the oxygen partial pressure in the reaction system and the total reaction pressure are in the range of 1 to 50 atmospheres, and the oxygen concentration in the exhaust gas is in the range of 1 to 8%. As the reaction method, any of a batch method, a semi-continuous method, and a continuous method can be employed, but a continuous method is preferably used.
かくして酸化反応を行つた結果、本発明におけ
る酸化反応混合物の反応母液中には反応で酢酸か
ら副生した酢酸メチルが含まれている。従来、テ
レフタル酸を分離した反応母液は、次いで蒸留分
離して水分を除去した後、溶媒として再使用して
いる。この場合、反応母液中の酢酸メチルは水分
と共に留出し、廃棄されていた。本発明では、こ
の微量の酢酸を含む水−酢酸メチルを蒸留して酢
酸メチルの少くとも一部、好ましくはほぼ全量を
回収し、これを前記酢酸を微量含む水の抽出溶媒
に使用するものである。 As a result of performing the oxidation reaction in this manner, the reaction mother liquor of the oxidation reaction mixture in the present invention contains methyl acetate produced as a by-product from acetic acid in the reaction. Conventionally, the reaction mother liquor from which terephthalic acid has been separated is then distilled to remove water and then reused as a solvent. In this case, methyl acetate in the reaction mother liquor was distilled out together with water and discarded. In the present invention, this water containing a trace amount of acetic acid-methyl acetate is distilled to recover at least a portion, preferably almost the entire amount, of the methyl acetate, and this is used as an extraction solvent for the water containing a trace amount of acetic acid. be.
以下、図面を参照しつつ本発明を説明する。 The present invention will be described below with reference to the drawings.
第１図は本発明の一実施態様のフローを示す図
である。 FIG. 1 is a diagram showing the flow of one embodiment of the present invention.
酸化反応で得られるスラリー状の酸化反応生成
物からテレフタル酸を分離した反応母液１を先
ず、塔頂90〜110℃、塔底110〜130℃の脱水蒸留
塔２で蒸留することにより、塔下部から酢酸３を
回収し、塔上部から水を主体とする混合液４を留
出せしめる。この混合液４中には微量の酢酸およ
び酢酸メチルが含まれているが、微量であるた
め、通常は分液せずに単相になつている。尚、反
応母液１については、常圧下、例えば120〜150℃
で蒸留して酢酸−水−酢酸メチル混合蒸気を蒸発
させ、脱水蒸留塔に供給する方法でもよい。次い
で、混合液４を常法により、液−液抽出塔５の上
部に導入し、抽出塔下部に後述する方法にて回収
した酢酸メチルを主体とする抽出溶媒６を供給
し、相互に向流接触させることにより、塔上部よ
り酢酸を含有する酢酸メチル７を得る。このよう
にして得た酢酸メチル７を、例えば、塔頂50〜65
℃、塔底90〜110℃の蒸留塔８で蒸留することに
より、酢酸９を分離取得し、例えば、脱水蒸留塔
２で得られた酢酸３と共に回収する。蒸留分離し
た酢酸メチル１０は、通常、全量ないしほぼ全量
抽出溶媒として活用する。一方、抽出塔底部から
得られる水１１の中には溶解度に相当する酢酸メ
チルを含有する為、この混合物を蒸留塔１２で前
記同様、蒸留することにより、塔頂より酢酸メチ
ル１３を回収することができる。このようにして
得た酢酸メチルは前記同様、通常、全量ないしほ
ぼ全量抽出溶媒として活用できるが、本発明の場
合、酢酸メチルが次々と副生される為、敢えて全
量回収する必要はない。また、本発明を実施する
場合、酢酸メチルの沸点が低い為、低温廃熱の回
収が容易であり、第２図に示すように、抽出塔上
部から得られる酢酸を含有する酢酸メチル７を熱
交換器１５を介して脱水蒸留塔２の底部液３の熱
を有効に回収すると、工業的に更に有利である。
また、酢酸メチルについては、液相酸化反応にお
いて発生するガスの中にも酢酸メチルが含まれて
いるので、この酢酸メチルを酢酸と接触させ、ガ
ス中に含まれる副生酢酸メチルのほぼ全量を酢酸
に吸収させて回収し、蒸留塔で蒸留分離の後、抽
出溶媒として活用するることや、液相酸化反応に
おいて発生するガスを凝縮器によつて得れる凝縮
液に含まれる酢酸メチルを蒸留塔で蒸留分離の
後、抽出溶媒として活用することも可能である。 The reaction mother liquor 1 from which terephthalic acid has been separated from the slurry-like oxidation reaction product obtained in the oxidation reaction is first distilled in a dehydration distillation column 2 at a temperature of 90 to 110°C at the top of the column and 110 to 130°C at the bottom of the column. Acetic acid 3 is recovered from the column, and a mixed liquid 4 mainly consisting of water is distilled from the upper part of the column. This mixed solution 4 contains a trace amount of acetic acid and methyl acetate, but because the amount is so small, it is usually made into a single phase without being separated. Regarding the reaction mother liquor 1, under normal pressure, for example, 120 to 150 °C
Alternatively, a mixed vapor of acetic acid-water-methyl acetate may be evaporated and supplied to a dehydration distillation column. Next, the mixed liquid 4 is introduced into the upper part of the liquid-liquid extraction tower 5 by a conventional method, and the extraction solvent 6 mainly composed of methyl acetate recovered by the method described later is supplied to the lower part of the extraction tower, and the mixture is made to flow countercurrently. By contacting, methyl acetate 7 containing acetic acid is obtained from the upper part of the column. The methyl acetate 7 thus obtained is, for example,
By distilling in the distillation column 8 at a temperature of 90 to 110[deg.] C., the acetic acid 9 is separated and collected, for example, together with the acetic acid 3 obtained in the dehydration distillation column 2. The methyl acetate 10 separated by distillation is usually used in its entirety or almost entirely as an extraction solvent. On the other hand, since the water 11 obtained from the bottom of the extraction column contains methyl acetate corresponding to the solubility, this mixture is distilled in the distillation column 12 in the same manner as described above to recover methyl acetate 13 from the top of the column. I can do it. As described above, methyl acetate obtained in this manner can normally be used as an extraction solvent in all or almost all amount, but in the case of the present invention, since methyl acetate is successively produced as a by-product, it is not necessary to recover the entire amount. Furthermore, when carrying out the present invention, since the boiling point of methyl acetate is low, it is easy to recover low-temperature waste heat, and as shown in Figure 2, methyl acetate 7 containing acetic acid obtained from the upper part of the extraction column is heated. It is further industrially advantageous to effectively recover the heat of the bottom liquid 3 of the dehydration distillation column 2 via the exchanger 15.
Regarding methyl acetate, since methyl acetate is also included in the gas generated in the liquid phase oxidation reaction, almost all of the by-product methyl acetate contained in the gas is removed by contacting this methyl acetate with acetic acid. Methyl acetate contained in the condensate obtained from the gas generated in the liquid phase oxidation reaction by a condenser can be distilled. After distillation separation in a column, it can also be used as an extraction solvent.
＜実施例＞ 以下実施例により本発明を具体的に説明する。<Example> The present invention will be specifically explained below using Examples.
実施例 １
パラキシレンを酢酸溶媒中、触媒として酢酸コ
バルトを、反応促進剤としてパラアルデヒドを用
い、温度120℃、圧力20Kg／cm2Ｇの条件下で液相
空気酸化して粗テレフタル酸を得た。Example 1 Crude terephthalic acid was obtained by liquid phase air oxidation of para-xylene in an acetic acid solvent using cobalt acetate as a catalyst and para-aldehyde as a reaction accelerator at a temperature of 120°C and a pressure of 20 kg/cm 2 G. Ta.
得られたテレフタル酸混合スラリーを０Kg／cm2
Ｇに減圧し、混合物スラリーの蒸留潜熱により
120℃から105℃に冷却せしめた。冷却後の混合物
スラリーは遠心分離機により母液と分離しテレフ
タル酸結晶を得た。次に分離母液を塔頂100℃、
塔底120℃の脱水蒸留塔に導入し、塔下部から酢
酸を回収すると共に塔上部から水を主体とする混
合液（酢酸1.4％および酢酸メチル1.77％を含む）
を得た。 The obtained terephthalic acid mixed slurry was 0Kg/cm 2
Due to the latent heat of distillation of the mixture slurry,
It was cooled from 120°C to 105°C. The cooled mixture slurry was separated from the mother liquor using a centrifuge to obtain terephthalic acid crystals. Next, the separated mother liquor was heated to 100℃ at the top of the column.
The bottom of the column is introduced into a dehydration distillation column at 120°C, and acetic acid is recovered from the bottom of the column, while a mixed liquid mainly consisting of water (containing 1.4% acetic acid and 1.77% methyl acetate) is released from the top of the column.
I got it.
以下、図面を参照しつつ本実施例を説明する。 The present embodiment will be described below with reference to the drawings.
第３図に従つて、抽出、溶媒回収からなる操作
を行つた。 According to FIG. 3, operations consisting of extraction and solvent recovery were performed.
先ず、上記混合液１４を１６を経由し、塔径
700mmφ、充填高さ６ｍの蒸留塔１２に導入し、
塔頂から酢酸メチル１３を回収する。回収した酢
酸メチル１３は、受そう１７に受入れ貯留させ、
該酢酸メチルを抽出塔５に充満させた。抽出塔は
塔径1000mmφ、充填高さが４ｍである。次に、抽
出塔の５の下から50℃に設定した酢酸メチル６を
7.5m3／Ｈ、上部に脱水蒸留塔から留出した酢酸
および酢酸メチルを含む水を主体とする混合液４
を50℃に設定して、５m3／Ｈ供給した。抽出塔５
の最下部からは溶解度に相当する酢酸メチルを含
有した水１１（以下、抽残相）を得、抽出塔の最
上部からは酢酸を抽出した酢酸メチル７（以下、
抽出相）を得た。この両液をそれぞれ１２およ
び、塔径1000mmφ、充填高さ６ｍの蒸留塔８に供
給し、酢酸メチル１０，１３を精製回収した。水
を主体とする混合液４を供給して12時間後、蒸留
塔１２の底部液１４に含まれる酢酸濃度を測定し
たところ0.17％であつた。また、抽出相と抽残相
との分離界面も良好であり、運転操作上は問題は
なかつた。 First, the mixed liquid 14 is passed through 16, and the column diameter is
Introduced into a distillation column 12 with a diameter of 700 mm and a filling height of 6 m,
Methyl acetate 13 is recovered from the top of the column. The recovered methyl acetate 13 is received and stored in a receiving tank 17,
The extraction column 5 was filled with the methyl acetate. The extraction column has a diameter of 1000 mm and a filling height of 4 m. Next, methyl acetate 6 set at 50℃ was added from below 5 of the extraction tower.
7.5m 3 /H, a mixed liquid mainly consisting of water containing acetic acid and methyl acetate distilled from the dehydration distillation column 4 in the upper part.
was set at 50°C, and 5 m 3 /H was supplied. Extraction tower 5
From the bottom of the column, water 11 (hereinafter referred to as raffinate phase) containing methyl acetate corresponding to the solubility is obtained, and from the top of the extraction column, methyl acetate 7 from which acetic acid has been extracted (hereinafter referred to as raffinate phase) is obtained.
Extract phase) was obtained. These two liquids were respectively supplied to distillation column 12 and distillation column 8 having a column diameter of 1000 mmφ and a packing height of 6 m, and methyl acetate 10 and 13 were purified and recovered. Twelve hours after supplying the mixed liquid 4 mainly consisting of water, the acetic acid concentration contained in the bottom liquid 14 of the distillation column 12 was measured and found to be 0.17%. Furthermore, the separation interface between the extraction phase and the raffinate phase was also good, and there were no problems in operation.
＜発明の効果＞
本発明によれば、脱水蒸留塔の留出水に微量含
まれる酢酸までも回収する事ができる。この結
果、留出水と共に廃棄されていた酢酸の損失が著
しく低下する。しかも、反応母液中の副生酢酸メ
チルを回収し抽出溶媒として活用するので、系が
複雑になることもなく、回収再使用が容易であ
り、工業的メリツトは大きい。その為、酢酸原単
位が低くなり、極めて経済的で工業的に有利な方
法を提供できた。<Effects of the Invention> According to the present invention, even trace amounts of acetic acid contained in distilled water from a dehydration distillation column can be recovered. As a result, the loss of acetic acid, which would have been discarded together with distilled water, is significantly reduced. Moreover, since the by-product methyl acetate in the reaction mother liquor is recovered and utilized as an extraction solvent, the system is not complicated and can be easily recovered and reused, which has great industrial merits. Therefore, the basic unit of acetic acid was reduced, and an extremely economical and industrially advantageous method could be provided.
第１図および第２図は本発明の一実施態様を示
すフローであり、また、第３図は本実施例で使用
したフローであり、図中の数字および文字は次の
ことを示す。
２……脱水蒸留塔、５……抽出塔、８，１２…
…酢酸メチル回収塔、１５……熱交換器、１７…
…酢酸メチル受そう。
1 and 2 are flows showing one embodiment of the present invention, and FIG. 3 is a flow used in this embodiment. Numbers and letters in the figures indicate the following. 2... Dehydration distillation column, 5... Extraction column, 8, 12...
...Methyl acetate recovery tower, 15... Heat exchanger, 17...
...I'll take methyl acetate.
Claims (1)
子状酸素含有ガスで液相酸化してテレフタル酸を
製造する方法によつて得られるスラリー状の酸化
反応生成物からテレフタル酸を分離した反応母液
から酢酸を回収するにあたり、該反応母液を脱水
蒸留塔に導入して、塔下部から酢酸を回収し、塔
上部から水を主体とし、酢酸−酢酸メチルを含む
混合液を留出せしめた後、該混合液中に微量含ま
れる酢酸を、液相酸化反応で酢酸から副生した回
収酢酸メチルを主体とする抽出溶媒を用いて液−
液抽出することにより回収することを特徴とする
酢酸の回収方法。 ２ 酢酸メチルを主体とする抽出溶媒が液相酸化
反応において発生するガスに含まれる酢酸メチル
のほぼ全量を回収したものを含有する特許請求の
範囲第１項記載の酢酸の回収方法。[Scope of Claims] 1. Terephthalic acid from a slurry-like oxidation reaction product obtained by a method of producing terephthalic acid by liquid-phase oxidation of para-xylene with a molecular oxygen-containing gas in the presence of a catalyst in an acetic acid solvent. To recover acetic acid from the reaction mother liquor separated, the reaction mother liquor is introduced into a dehydration distillation column, acetic acid is recovered from the lower part of the column, and a mixture mainly composed of water and containing acetic acid and methyl acetate is distilled from the upper part of the column. After the mixture is extracted, the trace amount of acetic acid contained in the mixture is extracted into a liquid using an extraction solvent mainly composed of recovered methyl acetate, which is a by-product from acetic acid in a liquid phase oxidation reaction.
A method for recovering acetic acid, characterized by recovering it by liquid extraction. 2. The method for recovering acetic acid according to claim 1, wherein the extraction solvent mainly containing methyl acetate contains a solvent obtained by recovering almost the entire amount of methyl acetate contained in the gas generated in the liquid phase oxidation reaction.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP30378386A JPS63156744A (en) | 1986-12-22 | 1986-12-22 | Recovery of acetic acid |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP30378386A JPS63156744A (en) | 1986-12-22 | 1986-12-22 | Recovery of acetic acid |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS63156744A JPS63156744A (en) | 1988-06-29 |
| JPH041734B2 true JPH041734B2 (en) | 1992-01-14 |
Family
ID=17925233
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP30378386A Granted JPS63156744A (en) | 1986-12-22 | 1986-12-22 | Recovery of acetic acid |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS63156744A (en) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW360636B (en) * | 1993-07-12 | 1999-06-11 | Glitsch | Method and apparatus for recovering acetic acid from aqueous streams |
| MY142126A (en) * | 2003-10-02 | 2010-09-15 | Mitsubishi Gas Chemical Co | Process for producing high-purity terephthalic acid |
| WO2006109999A1 (en) * | 2005-04-14 | 2006-10-19 | Amtpacific Co., Ltd. | Recovering method of acetic acid from effluent of terephthalic acid production process |
| CN103012102B (en) * | 2011-09-27 | 2014-09-17 | 中国石油化工股份有限公司 | Method of recovering acetic acid and water in production of aromatic carboxylic acid |
| CN104874196B (en) * | 2015-03-26 | 2016-09-14 | 南京师范大学 | A kind of method processing sodium and ammonium acetate salt-diazonium Organic substance-methanol-water mixed solution |
| CN105001073B (en) * | 2015-07-02 | 2017-06-20 | 中国石油天然气集团公司 | Low energy consumption material consumption, the PTA production methods and system of few waste discharge |
| JP6943131B2 (en) * | 2016-10-12 | 2021-09-29 | 三菱ケミカル株式会社 | Manufacturing method and equipment for organic carboxylic acid aqueous solution |
-
1986
- 1986-12-22 JP JP30378386A patent/JPS63156744A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS63156744A (en) | 1988-06-29 |
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